Control of the Solid-State Chiral Optical Properties of a Supramolecular Organic Fluorophore Containing 4-(2-Arylethynyl)-Benzoic Acid

The solid‐state chiral optical properties of a 4‐(2‐arylethynyl)‐benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the arylethynyl group of the achiral 4‐(2‐arylethynyl)‐benzoic acid component molecule rather than the chirality of the amine component molecule. So so...

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Veröffentlicht in:Chemistry, an Asian journal an Asian journal, 2011-04, Vol.6 (4), p.1092-1098
Hauptverfasser: Nishiguchi, Noriaki, Kinuta, Takafumi, Nakano, Yoko, Harada, Takunori, Tajima, Nobuo, Sato, Tomohiro, Fujiki, Michiya, Kuroda, Reiko, Matsubara, Yoshio, Imai, Yoshitane
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Sprache:eng
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Zusammenfassung:The solid‐state chiral optical properties of a 4‐(2‐arylethynyl)‐benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the arylethynyl group of the achiral 4‐(2‐arylethynyl)‐benzoic acid component molecule rather than the chirality of the amine component molecule. So solid crew: The solid‐state CD and CPL properties of a 4‐(2‐arylethynyl)‐benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the arylethynyl group of the achiral 4‐(2‐arylethynyl)‐benzoic acid component molecule.
ISSN:1861-4728
1861-471X
DOI:10.1002/asia.201000780